Anke Abt

Anke Abt Email and Phone Number

Qualitätsmanagement, Regulations und Prozess-Digitialisierung @ 3R LifeScience GmbH
Berlin, DE
Anke Abt's Location
Berlin, Berlin, Germany, Germany
Anke Abt's Contact Details

Anke Abt work email

Anke Abt personal email

n/a
About Anke Abt

I am a process analyst and expert in making processes work 😉Let's be honest - many companies currently face: ❌ a lot of time is spent searching for necessary information and documents❌ Information is not documented or is not accessible to those who need it❌ Decisions are delayed or in many cases not made at all due to a lack of information💡 THE SOLUTION: Documented processes (SOPs) that describe clearly the scope of work, responsibilities and in- and output of information and actions to make processes work.THEREFORE: I can help you to bring structure to your existing processes and define and align interfaces, so relevant information and process data is made available to your organisation. So if you want to know✔ how to create processes that allow you to generate information ✔ how to provide information in a timely and focused manner✔ how you can make faster and better decisions as a result✔ create a smart and lean QM system in parallelWe should talk!Just send me a message directly here via Linkedin.And we'll bring your organisation to make faster and better decisions.

Anke Abt's Current Company Details
3R LifeScience GmbH

3R Lifescience Gmbh

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Qualitätsmanagement, Regulations und Prozess-Digitialisierung
Berlin, DE
Employees:
7
Anke Abt Work Experience Details
  • 3R Lifescience Gmbh
    Qualitätsmanagement, Regulations Und Prozess-Digitialisierung
    3R Lifescience Gmbh
    Berlin, De
  • 3R Lifescience Gmbh
    Quality Management And Regulations
    3R Lifescience Gmbh Jul 2020 - Present
    Berlin, Deutschland
    Development and implementation of structures and MDR-compliant processes for safe and effective medical devicesDevelopment, implementation and maintenance of QM systems according to ISO 13485 for complete quality management systemsImplementation of the EU regulation MDR 2017/745:- Review and gap analysis of existing technical documents- Preparation and adaptation of technical documentsOptimisation of R&D, QM and regulatory interfaces for a target-oriented development of medical devicesDevelopment of process landscapes and creation and review of Quality Manuals and SOPsPreparation of internal and external audits and planning of measuresCAPA processes and change management
  • Dreve Prodimed Gmbh
    Quality Manager
    Dreve Prodimed Gmbh 2018 - 2020
    Unna, Nordrhein-Westfalen, Deutschland
    Development, optimisation and maintenance of ISO 13485 quality management processes as well as establishment of MDR-compliant technical documentationImplementation of MDR-compliant processesAudit support: MDSAP, ISO 13485Preparation of the technical documentationConducting internal auditsTraining and instruction of employeesCoordination of the digitalisation of quality-relevant processes
  • Ranova Überörtliche Gemeinschaftspraxis Für Radiologie Und Nuklearmedizin Gbr
    Quality Manager, Head Of Quality Management
    Ranova Überörtliche Gemeinschaftspraxis Für Radiologie Und Nuklearmedizin Gbr 2012 - 2018
    Unna
    Merging of 13 practice locations with different QM systems to form an overall QM system according to ISO 9001Strategic development of the QM system with the aim of scalability Consulting and reporting to the managementInterface management between the group of practices and the quality departments of the cooperating hospitalsconducting internal audits Support of certification audits as QMBControl and monitoring of error and complaint managementRequirements management for the implementation of internal knowledge data and for the administration of devices, testing/measuring equipmentTraining and instruction of shareholders and employeesMonitoring and supervision of measures from audits on compliance topics (data protection, specialist for occupational safety, hygiene, occupational medicine)Development and implementation of a uniform and scalable inspection and instruction concept in the areas of occupational safety, data protection, hygiene and occupational medical care for 13 radiology practices
  • Richts & Chedor Gmbh & Co. Kg
    Orthopädietechnikerin/-Meisterin, Qmb
    Richts & Chedor Gmbh & Co. Kg 2002 - 2012
    Werl
    Production of special medical-technical products and quality management representatives Manufacture of special medical technology productsField service, customer serviceSelection and fitting of orthopaedic aidsQuality Management Representative: Establishment of a QM system according to ISO 13585 and ISO 9001

Anke Abt Education Details

  • Meisterschule Für Orthopädietechnik
    Meisterschule Für Orthopädietechnik
    Orthopädietechnikmeister
  • Ausbildung Zur Orthopädietechnikerin
    Ausbildung Zur Orthopädietechnikerin
    Orthopädietechnikerin

Frequently Asked Questions about Anke Abt

What company does Anke Abt work for?

Anke Abt works for 3r Lifescience Gmbh

What is Anke Abt's role at the current company?

Anke Abt's current role is Qualitätsmanagement, Regulations und Prozess-Digitialisierung.

What is Anke Abt's email address?

Anke Abt's email address is an****@****ence.de

What schools did Anke Abt attend?

Anke Abt attended Meisterschule Für Orthopädietechnik, Ausbildung Zur Orthopädietechnikerin.

Who are Anke Abt's colleagues?

Anke Abt's colleagues are Sarah S., Dr.-Ing. Janin Leuckert, Michaela Hajek.

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